Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Could My Husband Have Celiac Disease


AnnaH

Recommended Posts

AnnaH Newbie

I cut my grain and legumes consumption about 2 years ago in an attempt to reduce my cholesterol.

After a couple of weeks I realized that I felt overall better on this diet: my energy level increased, the frequency of my migraines decreased, digestive problems (bloating, gas) has pretty much disappeared, so I stayed with the diet. In 6 months or so my decades-old depression lifted, though at that time I did not connect that to my diet. I was not fully gluten-free, I did not think I could have celiac.

This spring I started to notice that my reaction to eating wheat is getting more and more severe. I googled the subject and realized I had quite a few celiac symptoms. Around the same time I learned that my brother has developed classic celiac symptoms in the last year. That was enough for me to turn my household gluten-free. My husband just went along, he eats what he gets at home and since he always wants to loose weight he did not mind that we mainly eat vegetables and fish. I was never careful with CC and even allowed myself an occasional beer, but we both eat very limited amount of gluten in the last 2 months.

Not long ago I decided I'd like a firm diagnosis if I have celiac disease or only gluten intolerance. I saw a GI doctor who told me to start eating gluten and schedule an endoscopy in 2 weeks. DH welcomed the opportunity to have pizza, pasta, fresh bread at home. Our first glutened meal was 4 days ago. I could not even finish it, had to run to the bathroom. DH enjoyed every bread crumb of it. Next day I could hardly drag myself around, had stomach issues (and C ever since). DH had a blast eating pizza.

Next day I am even worse, DH decides to go for a long bike ride. He comes home exhausted: his muscles hurt, he had to push his bike up hills he usually clears without problem, he is out for the rest of the day. Following day we are both tired, DH says that maybe he will have just salad and not pasta for lunch. But he cannot resist, eats the pasta anyhow. That was yesterday. Well, DH spent the night in the bathroom. His D is like water, his stomach cramps are intense. Meanwhile I am still C; he jokes that if we combine our symptoms we are just right. I grit my teeth and tell him that I think he might be the celiac of the family.

DH did not appreciate my suggestion. He says I act like I have a hammer and now everything is a nail. (I have the tendency to do that.) And indeed, what is the probability that both of us have celiac disease? Any suggestions of how to proceed from here? Should I convince him to get a GI appointment and get tested? Or am I just projecting my prejudices on him?


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Skylark Collaborator

You planted a seed. Stand back and see if it grows. It's very easy to label everything under the sun gluten intolerance, and if you don't give him space to start looking at his own symptoms he'll just keep fighting you. It's possible your poor hubby just had a round of flu, so keep an eye over the next few days.

cassP Contributor

you both could yes. you never know really... and you cant always tell by the symptoms... you might as well BOTH get tested- it cant hurt really.. its better than not knowing and possibly getting really sick in the future.

and even if you both come up negative- the fact that you feel better OFF gluten should motivate you. some Celiacs dont have any gut issues- and some NONCeliacs can feel awful or even develop Crohns or Colitis....

its just so tricky sometimes.

enjoy the pizza for me :(

ravenwoodglass Mentor

It does sound like you are both positive to the gluten challenge even though your reactions were a bit different.

On the endoscopy, if you have been really gluten light for a while you need more than 2 weeks back on a gluten diet. Most advise at least 2 months. If you biopsy after just 2 weeks your chances of a false negative are pretty high. Even on a full gluten diet you still have a chance of a false negative. You don't need a doctors permission to be gluten free but if you really want a doctor derived diagnosis then you may want to move the biopsy back another 6 weeks.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,398
    • Most Online (within 30 mins)
      7,748

    Megannnnn
    Newest Member
    Megannnnn
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Scott Adams
    • Scott Adams
      I had the same thing happen to me at around your age, and to this day it's the most painful experience I've ever had. For me it was the right side of my head, above my ear, running from my nerves in my neck. For years before my outbreak I felt a tingling sensation shooting along the exact nerves that ended up exactly where the shingles blisters appeared. I highly recommend the two shot shingles vaccine as soon as your turn 50--I did this because I started to get the same tingling sensations in the same area, and after the vaccines I've never felt that again.  As you likely know, shingles is caused by chicken pox, which was once though of as one of those harmless childhood viruses that everyone should catch in the wild--little did they know that it can stay in your nervous system for your entire life, and cause major issues as you age.
    • trents
    • Clear2me
      Thanks for the info. I recently moved to CA from Wyoming and in that western region the Costco and Sam's /Walmart Brands have many nuts and more products that are labeled gluten free. I was told it's because those products are packaged and processed  in different  plants. Some plants can be labeled  gluten free because the plant does not also package gluten products and they know that for example the trucks, containers equipment are not used to handle wheat, barely or Rye. The Walmart butter in the western region says gluten free but not here. Most of The Kirkland and Members Mark brands in CA say they are from Vietnam. That's not the case in Wyoming and Colorado. I've spoken to customer service at the stores here in California. They were not helpful. I check labels every time I go to the store. The stores where I am are a Sh*tshow. The Magalopoly grocery chain Vons/Safeway/Albertsons, etc. are the same. Fishers and Planters brands no longer say gluten free. It could be regional. There are nuts with sugar coatings and fruit and nut mixes at the big chains that are labeled gluten free but I don't want the fruit or sugar.  It's so difficult I am considering moving again. I thought it would be easier to find safe food in a more populated area. It's actually worse.  I was undiagnosed for most of my life but not because I didn't try to figure it out. So I have had all the complications possible. I don't have any spare organs left.  No a little gluten will hurt you. The autoimmune process continues to destroy your organs though you may not feel it. If you are getting a little all the time and as much as we try we probably all are and so the damage is happening. Now the FDA has pretty much abandoned celiacs. There are no requirements for labeling for common allergens on medications. All the generic drugs made outside the US are not regulated for common allergens and the FDA is taking the last gluten free porcine Thyroid med, NP Thyroid, off the market in 2026. I was being glutened by a generic levothyroxin. The insurance wouldn't pay for the gluten free brand any longer because the FDA took them all off their approved formulary. So now I am paying $147 out of pocket for NP Thyroid but shortly I will have no safe choice. Other people with allergies should be aware that these foreign generic pharmaceutical producers are using ground shellfish shell as pill coatings and anti-desicants. The FDA knows this but  now just waits for consumers to complain or die. The take over of Wholefoods by Amazon destroyed a very reliable source of good high quality food for people with allergies and for people who wanted good reliably organic food. Bezos thought  he could make a fortune off people who were paying alot for organic and allergen free food by substituting cheap brands from Thailand. He didn't understand who the customers were who were willing to pay more for that food and why. I went from spending hundreds to nothing because Bezo removed every single trusted brand that I was buying. Now they are closing Whole foods stores across the country. In CA, Mill Valley store (closed July 2025) and the National Blvd. store in West Los Angeles (closed October 2025). The Cupertino store will close.  In recent years I have learned to be careful and trust no one. I have been deleberately glutened in a restaurant that was my favorite (a new employee). The Chef owner was not in the kitchen that night. I've had  a metal scouring pad cut up over my food.The chain offered gluten free dishes but it only takes one crazy who thinks you're a problem as a food fadist. Good thing I always look. Good thing they didn't do that to food going to a child with a busy mom.  I give big tips and apologize for having to ask in restaurants but mental illness seem to be rampant. I've learn the hard way.          I don't buy any processed food that doesn't say gluten free.  I am a life long Catholic. I worked for the Church while at college. I don't go to Church anymore because the men at the top decided Jesus is gluten. The special hosts are gluten less not gluten free. No I can't drink wine after people with gluten in their mouth and a variety of deadly germs. I have been abandoned and excluded by my Church/Family.  Having nearly died several times, safe food is paramount. If your immune system collapses as mine did, you get sepsis. It can kill you very quickly. I spent 5 days unconscious and had to have my appendix and gall bladder removed because they were necrotic. I was 25. They didn't figure out I had celiac till I was 53. No one will take the time to tell you what can happen when your immune system gets overwhelmed from its constant fighting the gluten and just stops. It is miserable that our food is processed so carelessly. Our food in many aspects is not safe. And the merging of all the grocery chains has made it far worse. Its a disaster. Krogers also recently purchased Vitacost where I was getting the products I could no longer get at Whole Foods. Kroger is eliminating those products from Vitacost just a Bezos did from WF. I am looking for reliable and certified sources for nuts. I have lived the worst consequences of the disease and being exposed unknowingly and maliciously. Once I was diagnosed I learned way more than anyone should have to about the food industry.  I don't do gray areas. And now I dont eat out except very rarely.  I have not eaten fast food for 30 years before the celiac diagnosis. Gluten aside..... It's not food and it's not safe.  No one has got our backs. Sharing safe food sources is one thing we can do to try to be safe.        
    • Mmoc
      Thank you kindly for your response. I have since gotten the other type of bloods done and am awaiting results. 
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.